High levels of SARS-CoV-2–specific T cells with restricted functionality in severe courses of COVID-19

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Abstract

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  1. SciScore for 10.1101/2020.07.08.20148718: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    Institutional Review Board StatementIRB: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.
    Consent: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.
    Randomizationnot detected.
    Blindingnot detected.
    Power Analysisnot detected.
    Sex as a biological variablenot detected.

    Table 2: Resources

    Antibodies
    SentencesResources
    Quantitation of lymphocyte populations: Quantitation and characterization of lymphocyte subpopulations was performed on 100 µL of heparinized whole blood as described before 36 using monoclonal antibodies towards CD3 (clone SK7), CD4 (clone SK3), CD8 (clone RPA-T8 and SK1), CD16 (clone 3G8), CD19 (clone HIB19), CD27 (clone L128), CD38 (clone HB7), CD56 (clone B159), cytotoxic T lymphocyte antigen 4 (CTLA-4, clone BNI3), IgD (clone IA6-2) and programmed cell death 1 (PD-1, clone MIH4, all from BD Biosciences).
    CD4
    suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)
    CD8
    suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)
    CD16
    suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)
    CD19
    suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)
    CD38
    suggested: (RayBiotech Cat# CS-11-0123, RRID:AB_1228026)
    CTLA-4
    suggested: None
    IgD
    suggested: None
    PD-1
    suggested: None
    Differentiation status of CD19-positive B-cells was assessed using antibodies against IgD and CD27.
    antibodies against IgD
    suggested: None
    CD27
    suggested: None
    NK cells were identified using antibodies towards CD3, CD16 and CD56 and quantified as CD3 negative/CD16/CD56 positive lymphocytes.
    CD3
    suggested: None
    CD56
    suggested: None
    Analysis of SARS-CoV-2 specific antibodies: SARS-CoV-2 specific antibodies were quantified from heparinized plasma samples using an IgG and IgA assay coated with recombinant S1-domain of SARS-CoV-2 spike protein antigen according to the manufacturer’s instructions (Euroimmun, Lübeck, Germany).
    SARS-CoV-2 spike protein
    suggested: None
    An unpaired non-parametric Kruskall-Wallis test with Dunn’s post test was used to analyze differences for lymphocyte subpopulations, T-cell and antibody levels as wells as PD-1, CTLA-4 and Ki67 of total T-cells among the three groups.
    PD-1, CTLA-4
    suggested: (Thermo Fisher Scientific Cat# EPX140-15803-901, RRID:AB_2576106)
    Software and Algorithms
    SentencesResources
    Statistical analysis: Statistical analysis was carried out using GraphPad Prism 8.0 software using two-tailed tests.
    GraphPad Prism
    suggested: (GraphPad Prism, RRID:SCR_002798)

    Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).


    Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.

    Results from TrialIdentifier: No clinical trial numbers were referenced.


    Results from Barzooka: We found bar graphs of continuous data. We recommend replacing bar graphs with more informative graphics, as many different datasets can lead to the same bar graph. The actual data may suggest different conclusions from the summary statistics. For more information, please see Weissgerber et al (2015).


    Results from JetFighter: We did not find any issues relating to colormaps.


    Results from rtransparent:
    • Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
    • No protocol registration statement was detected.

    About SciScore

    SciScore is an automated tool that is designed to assist expert reviewers by finding and presenting formulaic information scattered throughout a paper in a standard, easy to digest format. SciScore checks for the presence and correctness of RRIDs (research resource identifiers), and for rigor criteria such as sex and investigator blinding. For details on the theoretical underpinning of rigor criteria and the tools shown here, including references cited, please follow this link.